B7-33

B7-33

Note:
  • USA MADE 2-7 days delivery
  • International 5-20 days delivery
Out of stock

Product Overview

A fundamental standard in cardiovascular and tissue remodeling research dictates that exploring advanced antifibrotic compounds requires complete structural integrity and verified chemical purity. The B7-33 formulation addresses these demanding benchmarks, serving as a highly purified synthetic peptide derivative engineered for precise in vitro and in vivo laboratory modeling of relaxin receptor dynamics. Each vial provides pure B7-33, stabilized as a vacuum freeze-dried (lyophilized) powder maintaining a verified purity profile of greater than 98%.

B7-33 is a functionally selective, single-chain synthetic peptide derived from the B-chain of human gene-2 relaxin (H2 relaxin). Unlike native H2 relaxin, which features a complex, dual-chain structure linked by disulfide bonds, B7-33 is a truncated, single-chain peptide containing the essential receptor-binding cassette. This engineered structural modification is a major asset: it simplifies the molecular architecture, significantly lowering manufacturing complexity while preserving the precise binding topology required to selectively activate target pathways.

Operating as a potent, non-promiscuous agonist, B7-33 binds preferentially to the Relaxin Family Peptide Receptor 1 (RXFP1). Upon binding, it activates beneficial pERK1/2 signaling cascades that drive matrix metalloproteinase (MMP) up-regulation and suppress pro-fibrotic transforming growth factor-beta (TGF-β) pathways. Crucially, B7-33 does not activate the cAMP-dependent signaling pathways associated with tumor growth or cross-react with insulin receptors. Documented research demonstrates that this selective mechanism effectively reduces collagen deposition, halts aberrant tissue remodeling, and promotes the breakdown of existing scar tissue. This provides researchers with a highly sophisticated model for investigating targeted organ fibrosis mitigation, vascular compliance, and wound healing dynamics within controlled environments.

Product Specifications

  • Form: Lyophilized (vacuum freeze-dried) powder
  • Purity: Greater than 98% (verified by HPLC analysis)
  • Peptide Architecture: Single-chain synthetic relaxin-like peptide
  • Primary Target: RXFP1 (Relaxin Family Peptide Receptor 1)
  • Primary Research Focus: Selective Antifibrotic Signaling, MMP Activation, and Tissue Remodeling

Container Specifications

The physical attributes of the storage vessel directly impact the shelf life of the compound. All research environments should utilize clean, chemically inert containers. Glass vials provide the highest level of protection against gas permeability and chemical interaction, though high-density polypropylene tubes serve as a valid alternative. Keep all stored peptides away from automatic frost-free freezers, as their internal defrost cycles create regular temperature swings that compromise peptide longevity.

Storage and Handling Protocols

Preserving the biological utility of a high-purity single-chain peptide requires strict adherence to precise environmental controls. Because the molecular bonds remain vulnerable to thermal, moisture-driven, and atmospheric degradation, researchers must follow standardized handling protocols to prevent structural breakdown.

Lyophilized Powder Preservation

Unopened, lyophilized vials must be kept in long-term cold storage at a stable temperature of -20°C. For extended storage timelines exceeding one year, maintaining a temperature of -80°C is highly recommended to completely arrest baseline molecular degradation. Vials should remain housed in sealed, light-shielded containers to prevent degradation from ultraviolet exposure and atmospheric moisture.

Before opening a vial or introducing a reconstitution solvent, allow the container to sit at room temperature until it fully equilibrates. Skipping this step introduces a substantial risk of moisture condensation forming on the cold powder, which immediately accelerates chemical breakdown.

Properly stored at -20°C, the lyophilized powder remains stable and viable for a period of 2 to 4 years.

For optimal preservation, utilize airtight glass vials equipped with PTFE-lined caps. If a vial is opened to remove fractional quantities, the remaining headspace should be flushed with an inert gas like dry nitrogen or argon before resealing to minimize oxidative risk across the peptide chain.

Reconstituted Solution Stability

Once transitioned into a liquid state, the peptide becomes significantly more fragile. Reconstituted B7-33 solutions must be kept under continuous refrigeration at 2-8°C and should be completely utilized within 30 days. If your experimental timeline requires keeping the liquid compound past this threshold, divide the freshly mixed solution into single-use aliquots immediately after reconstitution and freeze them at -20°C or -80°C.

To maintain maximum stability, employ sterile, neutral buffers or sterile water. Repeated freeze-thaw cycles must be strictly avoided, as the physical stress of phase changes causes structural shearing of the peptide chain.

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At PeptideHubs, scientific integrity and product reliability are at the core of everything we do. Each compound is manufactured and tested under strict quality control protocols to ensure consistency, purity, and performance for research applications.

However, if for any reason our product does not meet your research expectations, we offer a 60-day money-back guarantee — providing a risk-free procurement experience for qualified researchers and institutions.

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